EA012062B1 - Промышленный способ отделения диалкилкарбоната - Google Patents
Промышленный способ отделения диалкилкарбоната Download PDFInfo
- Publication number
- EA012062B1 EA012062B1 EA200800919A EA200800919A EA012062B1 EA 012062 B1 EA012062 B1 EA 012062B1 EA 200800919 A EA200800919 A EA 200800919A EA 200800919 A EA200800919 A EA 200800919A EA 012062 B1 EA012062 B1 EA 012062B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- column
- section
- distillation
- carbonate
- dialkyl carbonate
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 19
- 238000004821 distillation Methods 0.000 claims abstract description 149
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 73
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 72
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 65
- 238000009835 boiling Methods 0.000 claims abstract description 43
- 150000005676 cyclic carbonates Chemical class 0.000 claims abstract description 41
- 239000011541 reaction mixture Substances 0.000 claims abstract description 34
- 238000000926 separation method Methods 0.000 claims abstract description 29
- 238000000066 reactive distillation Methods 0.000 claims abstract description 28
- 150000002009 diols Chemical class 0.000 claims abstract description 25
- 238000001704 evaporation Methods 0.000 claims abstract description 20
- 230000008020 evaporation Effects 0.000 claims abstract description 20
- 239000007788 liquid Substances 0.000 claims abstract description 14
- 239000002815 homogeneous catalyst Substances 0.000 claims abstract description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 75
- 238000000034 method Methods 0.000 claims description 63
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 38
- 239000007858 starting material Substances 0.000 claims description 27
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 15
- 230000014509 gene expression Effects 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 5
- 238000010992 reflux Methods 0.000 claims description 4
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 33
- 239000000047 product Substances 0.000 description 26
- 239000000203 mixture Substances 0.000 description 23
- -1 alkylene carbonate Chemical compound 0.000 description 19
- 239000003054 catalyst Substances 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 229910052788 barium Inorganic materials 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 238000005809 transesterification reaction Methods 0.000 description 3
- AGBWDHTZUCGTAI-UHFFFAOYSA-N 1-(cycloundecen-1-yl)-3-diazocycloundecene Chemical compound [N-]=[N+]=C1CCCCCCCCC(C=2CCCCCCCCCC=2)=C1 AGBWDHTZUCGTAI-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 150000001251 acridines Chemical class 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical compound CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- RYSXWUYLAWPLES-MTOQALJVSA-N (Z)-4-hydroxypent-3-en-2-one titanium Chemical compound [Ti].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O RYSXWUYLAWPLES-MTOQALJVSA-N 0.000 description 1
- YOBOXHGSEJBUPB-MTOQALJVSA-N (z)-4-hydroxypent-3-en-2-one;zirconium Chemical compound [Zr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O YOBOXHGSEJBUPB-MTOQALJVSA-N 0.000 description 1
- KPOORJWULWXLPB-UHFFFAOYSA-N 1-(cyclononen-1-yl)-3-diazocyclononene Chemical compound [N-]=[N+]=C1CCCCCCC(C=2CCCCCCCC=2)=C1 KPOORJWULWXLPB-UHFFFAOYSA-N 0.000 description 1
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- LPCWIFPJLFCXRS-UHFFFAOYSA-N 1-ethylcyclopentan-1-ol Chemical compound CCC1(O)CCCC1 LPCWIFPJLFCXRS-UHFFFAOYSA-N 0.000 description 1
- ZSPTYLOMNJNZNG-UHFFFAOYSA-N 3-Buten-1-ol Chemical compound OCCC=C ZSPTYLOMNJNZNG-UHFFFAOYSA-N 0.000 description 1
- MWHLORMGUXPWLW-UHFFFAOYSA-N 4,4-diethylcyclohexan-1-ol Chemical compound CCC1(CC)CCC(O)CC1 MWHLORMGUXPWLW-UHFFFAOYSA-N 0.000 description 1
- DUFCMRCMPHIFTR-UHFFFAOYSA-N 5-(dimethylsulfamoyl)-2-methylfuran-3-carboxylic acid Chemical compound CN(C)S(=O)(=O)C1=CC(C(O)=O)=C(C)O1 DUFCMRCMPHIFTR-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- FVNAFOGXZVJPTL-UHFFFAOYSA-N C1(=CC=CC=C1)[Sn](OC)C1=CC=CC=C1 Chemical compound C1(=CC=CC=C1)[Sn](OC)C1=CC=CC=C1 FVNAFOGXZVJPTL-UHFFFAOYSA-N 0.000 description 1
- XEBVGEGFCWTBIF-UHFFFAOYSA-N C1CCNC1.C1=NC=CC2=CC=CC=C21 Chemical class C1CCNC1.C1=NC=CC2=CC=CC=C21 XEBVGEGFCWTBIF-UHFFFAOYSA-N 0.000 description 1
- ZALOHOLPKHYYAX-UHFFFAOYSA-L CO[Ti](Cl)(Cl)OC Chemical compound CO[Ti](Cl)(Cl)OC ZALOHOLPKHYYAX-UHFFFAOYSA-L 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- GCTFWCDSFPMHHS-UHFFFAOYSA-M Tributyltin chloride Chemical compound CCCC[Sn](Cl)(CCCC)CCCC GCTFWCDSFPMHHS-UHFFFAOYSA-M 0.000 description 1
- JJLKTTCRRLHVGL-UHFFFAOYSA-L [acetyloxy(dibutyl)stannyl] acetate Chemical compound CC([O-])=O.CC([O-])=O.CCCC[Sn+2]CCCC JJLKTTCRRLHVGL-UHFFFAOYSA-L 0.000 description 1
- INNSZZHSFSFSGS-UHFFFAOYSA-N acetic acid;titanium Chemical compound [Ti].CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O INNSZZHSFSFSGS-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- FHADSMKORVFYOS-UHFFFAOYSA-N cyclooctanol Chemical compound OC1CCCCCCC1 FHADSMKORVFYOS-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- ZNZBASDDVBURLC-UHFFFAOYSA-N dibutyl(diethoxy)stannane Chemical compound CCCC[Sn](OCC)(OCC)CCCC ZNZBASDDVBURLC-UHFFFAOYSA-N 0.000 description 1
- UDSMOEAHRBVXFA-UHFFFAOYSA-M dibutyl(phenoxy)tin Chemical compound CCCC[Sn](CCCC)OC1=CC=CC=C1 UDSMOEAHRBVXFA-UHFFFAOYSA-M 0.000 description 1
- ZXDVQYBUEVYUCG-UHFFFAOYSA-N dibutyltin(2+);methanolate Chemical compound CCCC[Sn](OC)(OC)CCCC ZXDVQYBUEVYUCG-UHFFFAOYSA-N 0.000 description 1
- CJOCCCWCYHQYPZ-UHFFFAOYSA-N diethoxy(diethyl)stannane Chemical compound CCO[Sn](CC)(CC)OCC CJOCCCWCYHQYPZ-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- XGZNHFPFJRZBBT-UHFFFAOYSA-N ethanol;titanium Chemical compound [Ti].CCO.CCO.CCO.CCO XGZNHFPFJRZBBT-UHFFFAOYSA-N 0.000 description 1
- 238000000895 extractive distillation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052949 galena Inorganic materials 0.000 description 1
- 229910021389 graphene Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 150000002611 lead compounds Chemical class 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- XCAUINMIESBTBL-UHFFFAOYSA-N lead(ii) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- ZEIWWVGGEOHESL-UHFFFAOYSA-N methanol;titanium Chemical compound [Ti].OC.OC.OC.OC ZEIWWVGGEOHESL-UHFFFAOYSA-N 0.000 description 1
- KJGLZJQPMKQFIK-UHFFFAOYSA-N methanolate;tributylstannanylium Chemical compound CCCC[Sn](CCCC)(CCCC)OC KJGLZJQPMKQFIK-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
- ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical compound CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- FYWSTUCDSVYLPV-UHFFFAOYSA-N nitrooxythallium Chemical compound [Tl+].[O-][N+]([O-])=O FYWSTUCDSVYLPV-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 150000002916 oxazoles Chemical class 0.000 description 1
- WKMKTIVRRLOHAJ-UHFFFAOYSA-N oxygen(2-);thallium(1+) Chemical compound [O-2].[Tl+].[Tl+] WKMKTIVRRLOHAJ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- WGPCGCOKHWGKJJ-UHFFFAOYSA-N sulfanylidenezinc Chemical compound [Zn]=S WGPCGCOKHWGKJJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- 150000003475 thallium Chemical class 0.000 description 1
- 150000003476 thallium compounds Chemical class 0.000 description 1
- 229910021515 thallium hydroxide Inorganic materials 0.000 description 1
- 229910003438 thallium oxide Inorganic materials 0.000 description 1
- YTQVHRVITVLIRD-UHFFFAOYSA-L thallium sulfate Chemical compound [Tl+].[Tl+].[O-]S([O-])(=O)=O YTQVHRVITVLIRD-UHFFFAOYSA-L 0.000 description 1
- 229940119523 thallium sulfate Drugs 0.000 description 1
- 229910000374 thallium(I) sulfate Inorganic materials 0.000 description 1
- DASUJKKKKGHFBF-UHFFFAOYSA-L thallium(i) carbonate Chemical compound [Tl+].[Tl+].[O-]C([O-])=O DASUJKKKKGHFBF-UHFFFAOYSA-L 0.000 description 1
- QGYXCSSUHCHXHB-UHFFFAOYSA-M thallium(i) hydroxide Chemical compound [OH-].[Tl+] QGYXCSSUHCHXHB-UHFFFAOYSA-M 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- SDTAGBUVRXOKAK-UHFFFAOYSA-N tributyl(ethoxy)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)OCC SDTAGBUVRXOKAK-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 229940057402 undecyl alcohol Drugs 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- YNPXMOHUBANPJB-UHFFFAOYSA-N zinc;butan-1-olate Chemical compound [Zn+2].CCCC[O-].CCCC[O-] YNPXMOHUBANPJB-UHFFFAOYSA-N 0.000 description 1
- WXKZSTUKHWTJCF-UHFFFAOYSA-N zinc;ethanolate Chemical compound [Zn+2].CC[O-].CC[O-] WXKZSTUKHWTJCF-UHFFFAOYSA-N 0.000 description 1
- JXNCWJJAQLTWKR-UHFFFAOYSA-N zinc;methanolate Chemical compound [Zn+2].[O-]C.[O-]C JXNCWJJAQLTWKR-UHFFFAOYSA-N 0.000 description 1
- 150000003755 zirconium compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/06—Preparation of esters of carbonic or haloformic acids from organic carbonates
- C07C68/065—Preparation of esters of carbonic or haloformic acids from organic carbonates from alkylene carbonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/06—Preparation of esters of carbonic or haloformic acids from organic carbonates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/009—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping in combination with chemical reactions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/14—Fractional distillation or use of a fractionation or rectification column
- B01D3/32—Other features of fractionating columns ; Constructional details of fractionating columns not provided for in groups B01D3/16 - B01D3/30
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B63/00—Purification; Separation; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/08—Purification; Separation; Stabilisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/96—Esters of carbonic or haloformic acids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005371643 | 2005-12-26 | ||
| PCT/JP2006/325089 WO2007074664A1 (ja) | 2005-12-26 | 2006-12-15 | ジアルキルカーボネートの工業的分離方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200800919A1 EA200800919A1 (ru) | 2008-08-29 |
| EA012062B1 true EA012062B1 (ru) | 2009-08-28 |
Family
ID=38217884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200800919A EA012062B1 (ru) | 2005-12-26 | 2006-12-15 | Промышленный способ отделения диалкилкарбоната |
Country Status (10)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105194899A (zh) * | 2015-10-16 | 2015-12-30 | 青岛科技大学 | 一种分离甲苯-异丁苯混合物的变径精馏装置及方法 |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20080049138A (ko) * | 2005-11-25 | 2008-06-03 | 아사히 가세이 케미칼즈 가부시키가이샤 | 디알킬카보네이트와 디올류를 공업적으로 제조하는 방법 |
| TWI334410B (en) | 2006-01-10 | 2010-12-11 | Asahi Kasei Chemicals Corp | Industrial process for production of high-purity diol |
| DE102009053370A1 (de) * | 2009-11-14 | 2011-05-19 | Bayer Materialscience Ag | Verfahren zur Reinigung von Dialkylcarbonaten |
| DE102010042934A1 (de) * | 2010-10-26 | 2012-04-26 | Bayer Materialscience Aktiengesellschaft | Verfahren zur kontinuierlichen Herstellung von Dialkylcarbonat |
| DE102010042936A1 (de) | 2010-10-26 | 2012-04-26 | Bayer Materialscience Aktiengesellschaft | Verfahren zur kontinuierlichen Herstellung von Dialkylcarbonat |
| US9656942B2 (en) * | 2012-10-15 | 2017-05-23 | Ube Industries, Ltd. | Method of manufacturing diethyl carbonate |
| CN107428669B (zh) | 2015-03-23 | 2021-07-16 | 沙特基础工业全球技术有限公司 | 用于生产碳酸芳基酯的整合的方法和装置 |
| KR20170129909A (ko) | 2015-03-23 | 2017-11-27 | 사빅 글로벌 테크놀러지스 비.브이. | 아릴 카보네이트의 제조를 위한 통합된 방법 및 장치 |
| JP7451771B2 (ja) * | 2021-01-08 | 2024-03-18 | 旭化成株式会社 | ジアルキルカーボネート類とジオール類を工業的に製造する方法 |
| WO2022230776A1 (ja) * | 2021-04-28 | 2022-11-03 | 旭化成株式会社 | ジアルキルカーボネートの製造方法、及びジアルキルカーボネートの製造装置 |
| KR102759664B1 (ko) * | 2021-11-30 | 2025-02-03 | 롯데케미칼 주식회사 | 카보네이트의 제조 방법 |
| CN118059788B (zh) * | 2024-04-17 | 2024-07-16 | 临涣焦化股份有限公司 | 一种碳酸二甲酯提纯脱轻装置及脱轻方法 |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06196464A (ja) * | 1992-12-25 | 1994-07-15 | San Seal:Kk | 半導体洗浄用炭酸ジエチルの製造方法 |
| JPH06228026A (ja) * | 1993-02-01 | 1994-08-16 | Mitsubishi Gas Chem Co Inc | メタノールとジメチルカーボネートの分離法 |
| JPH0725830A (ja) * | 1993-07-08 | 1995-01-27 | Daicel Chem Ind Ltd | 炭酸ジエステルの精製法及びその精製法によって得られた炭酸ジエステルを用いて製造したポリカーボネート |
| JPH09183744A (ja) * | 1995-10-31 | 1997-07-15 | Asahi Chem Ind Co Ltd | ジアルキルカーボネートおよびジオールの連続的製造法 |
| WO2000051954A1 (fr) * | 1999-03-03 | 2000-09-08 | Asahi Kasei Kabushiki Kaisha | Procede d'elaboration continue de carbonate dialcoyle et de diol |
| JP2000281630A (ja) * | 1999-03-26 | 2000-10-10 | Mitsubishi Chemicals Corp | 非対称ジアルキルカーボネートの製造方法 |
| JP2002371037A (ja) * | 2001-06-12 | 2002-12-26 | Mitsubishi Chemicals Corp | 高純度ジメチルカーボネートの製造方法 |
| JP2003342209A (ja) * | 2002-05-23 | 2003-12-03 | Mitsubishi Chemicals Corp | ジメチルカーボネート及びエチレングリコールの製造方法 |
| WO2005123638A1 (ja) * | 2004-06-17 | 2005-12-29 | Asahi Kasei Chemicals Corporation | ジアルキルカーボネートとジオールの製造方法 |
| WO2006001256A1 (ja) * | 2004-06-25 | 2006-01-05 | Asahi Kasei Chemicals Corporation | 芳香族カーボネートの工業的製造法 |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3642858A (en) | 1969-02-12 | 1972-02-15 | Dow Chemical Co | Carbonate synthesis from alkylene carbonates |
| US3803201A (en) | 1971-02-22 | 1974-04-09 | Dow Chemical Co | Synthesis of dimethyl carbonate |
| IT1034961B (it) | 1975-04-09 | 1979-10-10 | Snam Progetti | Procedimento per la preparazione di dialchilcarbonati |
| DE2740243A1 (de) | 1977-09-07 | 1979-03-15 | Bayer Ag | Verfahren zur herstellung von dialkylcarbonaten |
| DE2740251A1 (de) | 1977-09-07 | 1979-03-22 | Bayer Ag | Verfahren zur herstellung von dialkylcarbonaten |
| JPS5463023A (en) | 1977-10-26 | 1979-05-21 | Mitsubishi Chem Ind Ltd | Ester exchange of carbonate |
| JPS6022697B2 (ja) | 1978-05-16 | 1985-06-03 | 日曹油化工業株式会社 | ジアルキル炭酸エステルの製造法 |
| DE3146142A1 (de) | 1981-11-21 | 1983-06-01 | Henkel KGaA, 4000 Düsseldorf | Reaktionskolonne und dessen verwendung |
| JPS6431737A (en) | 1986-01-03 | 1989-02-02 | Texaco Development Corp | Manufacture of ethylene glycol and dimethyl carbonate |
| US4691041A (en) | 1986-01-03 | 1987-09-01 | Texaco Inc. | Process for production of ethylene glycol and dimethyl carbonate |
| US4661609A (en) | 1986-07-31 | 1987-04-28 | Texaco Inc. | Process for cosynthesis of ethylene glycol and dimethyl carbonate |
| US4734518A (en) | 1987-01-12 | 1988-03-29 | Texaco Inc. | Process for cosynthesis of ethylene glycol and dimethyl carbonate |
| JPH0737422B2 (ja) | 1987-03-26 | 1995-04-26 | 旭化成工業株式会社 | ジアルキルカ−ボネ−トの製造方法 |
| JP2529025B2 (ja) | 1990-11-29 | 1996-08-28 | 旭化成工業株式会社 | ジアルキルカ―ボネ―トとジオ―ル類の連続的製造法 |
| JPH0768180B2 (ja) | 1990-12-27 | 1995-07-26 | 旭化成工業株式会社 | ジアルキルカーボネートとジオール類の連続的製法 |
| DE4129316A1 (de) * | 1991-09-03 | 1993-03-04 | Bayer Ag | Verfahren zur kontinuierlichen herstellung von dialkylcarbonaten |
| DE4216121A1 (de) * | 1992-05-15 | 1993-11-18 | Bayer Ag | Verfahren zur kontinuierlichen Herstellung von Dialkylcarbonaten |
| JP4093607B2 (ja) | 1995-11-14 | 2008-06-04 | 旭化成ケミカルズ株式会社 | ジアルキルカーボネートおよびジオールの連続的製造方法 |
| JP3686086B2 (ja) | 1995-12-22 | 2005-08-24 | 旭化成ケミカルズ株式会社 | ジアルキルカ−ボネ−トとジオ−ルを連続的に製造する方法 |
| JPH09176061A (ja) | 1995-12-28 | 1997-07-08 | Asahi Chem Ind Co Ltd | ジアルキルカーボネートとジオールの連続的製造法 |
| US6346638B1 (en) * | 1998-06-10 | 2002-02-12 | Asahi Kasel Kabushiki Kaisha | Process for continuous production of dialkyl carbonate and diol |
| JP4467204B2 (ja) | 2001-04-13 | 2010-05-26 | 旭化成ケミカルズ株式会社 | ジアルキルカーボネートおよびジオールの製造方法 |
| JP4380102B2 (ja) | 2001-10-10 | 2009-12-09 | 三菱化学株式会社 | ジメチルカーボネートの製造方法 |
| WO2003006418A1 (fr) | 2001-07-10 | 2003-01-23 | Mitsubishi Chemical Corporation | Procede de production de dialkylcarbonate |
| US6573396B2 (en) | 2001-10-12 | 2003-06-03 | Exxonmobil Chemical Patents Inc. | Co-production of dialkyl carbonates and diols with treatment of hydroxy alkyl carbonate |
| JP2003300936A (ja) | 2002-04-09 | 2003-10-21 | Mitsui Chemicals Inc | ジアルキルカーボネートとグリコールの連続同時製造方法 |
| JP4424898B2 (ja) | 2002-10-08 | 2010-03-03 | 旭化成ケミカルズ株式会社 | ジアルキルカーボネートおよびジオールを製造する方法 |
| US20040104108A1 (en) | 2002-12-03 | 2004-06-03 | Mason Robert Michael | High capacity purification of thermally unstable compounds |
| CN100554241C (zh) | 2004-09-17 | 2009-10-28 | 旭化成化学株式会社 | 醇类副产物的工业分离方法 |
| JP4174541B2 (ja) | 2004-09-21 | 2008-11-05 | 旭化成ケミカルズ株式会社 | 副生アルコール類を工業的に分離する方法 |
| JP2006182683A (ja) | 2004-12-27 | 2006-07-13 | Asahi Kasei Chemicals Corp | ジオールおよびジアルキルカーボネートを製造する方法 |
| JP2006199643A (ja) | 2005-01-21 | 2006-08-03 | Asahi Kasei Chemicals Corp | ジオールおよびジアルキルカーボネートの製造方法 |
| JP2006206497A (ja) | 2005-01-28 | 2006-08-10 | Asahi Kasei Chemicals Corp | ジアルキルカーボネートおよびジオールを製造する方法 |
| KR20080049138A (ko) | 2005-11-25 | 2008-06-03 | 아사히 가세이 케미칼즈 가부시키가이샤 | 디알킬카보네이트와 디올류를 공업적으로 제조하는 방법 |
| US20090326257A1 (en) | 2005-12-12 | 2009-12-31 | Shinsuke Fukuoka | Process for industrially producing dialkyl carbonate and diol |
| TWI308911B (en) | 2005-12-13 | 2009-04-21 | Asahi Kasei Chemcials Corp | Process for industrially producing dialkyl carbonate and diol |
| TW200732291A (en) | 2005-12-14 | 2007-09-01 | Asahi Kasei Chemicals Corp | Process for production of dialkyl carbonate and diol in industrial scale and with high yield |
| TW200732290A (en) | 2005-12-16 | 2007-09-01 | Asahi Kasei Chemicals Corp | Industrial process for production of high-purity diaryl carbonate |
| TW200726745A (en) | 2005-12-16 | 2007-07-16 | Asahi Kasei Chemicals Corp | Industrial process for production of aromatic carbonate |
| CN101341114B (zh) | 2005-12-19 | 2012-07-25 | 旭化成化学株式会社 | 工业规模制备高纯度碳酸二苯酯的方法 |
| US20090264670A1 (en) | 2005-12-21 | 2009-10-22 | Shinsuke Fukuoka | Process for industrially producing dialkyl carbonate and diol |
| TW200738601A (en) | 2005-12-27 | 2007-10-16 | Asahi Kasei Chemicals Corp | Industrial process for production of dialkyl carbonate and diol |
| TW200738602A (en) | 2006-02-01 | 2007-10-16 | Asahi Kasei Chemicals Corp | Industrial process for producing high-purity diol |
-
2006
- 2006-12-07 TW TW095145698A patent/TWI314549B/zh active
- 2006-12-15 BR BRPI0620605A patent/BRPI0620605B1/pt active IP Right Grant
- 2006-12-15 KR KR1020087015406A patent/KR101002863B1/ko active Active
- 2006-12-15 EP EP06834816.8A patent/EP1967508B1/en active Active
- 2006-12-15 JP JP2007551903A patent/JP4260212B2/ja active Active
- 2006-12-15 IN IN869KON2008 patent/IN2008KN00869A/en unknown
- 2006-12-15 WO PCT/JP2006/325089 patent/WO2007074664A1/ja active Application Filing
- 2006-12-15 US US11/991,073 patent/US8049028B2/en active Active
- 2006-12-15 EA EA200800919A patent/EA012062B1/ru not_active IP Right Cessation
- 2006-12-15 CN CN2006800492531A patent/CN101346340B/zh active Active
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06196464A (ja) * | 1992-12-25 | 1994-07-15 | San Seal:Kk | 半導体洗浄用炭酸ジエチルの製造方法 |
| JPH06228026A (ja) * | 1993-02-01 | 1994-08-16 | Mitsubishi Gas Chem Co Inc | メタノールとジメチルカーボネートの分離法 |
| JPH0725830A (ja) * | 1993-07-08 | 1995-01-27 | Daicel Chem Ind Ltd | 炭酸ジエステルの精製法及びその精製法によって得られた炭酸ジエステルを用いて製造したポリカーボネート |
| JPH09183744A (ja) * | 1995-10-31 | 1997-07-15 | Asahi Chem Ind Co Ltd | ジアルキルカーボネートおよびジオールの連続的製造法 |
| WO2000051954A1 (fr) * | 1999-03-03 | 2000-09-08 | Asahi Kasei Kabushiki Kaisha | Procede d'elaboration continue de carbonate dialcoyle et de diol |
| JP2000281630A (ja) * | 1999-03-26 | 2000-10-10 | Mitsubishi Chemicals Corp | 非対称ジアルキルカーボネートの製造方法 |
| JP2002371037A (ja) * | 2001-06-12 | 2002-12-26 | Mitsubishi Chemicals Corp | 高純度ジメチルカーボネートの製造方法 |
| JP2003342209A (ja) * | 2002-05-23 | 2003-12-03 | Mitsubishi Chemicals Corp | ジメチルカーボネート及びエチレングリコールの製造方法 |
| WO2005123638A1 (ja) * | 2004-06-17 | 2005-12-29 | Asahi Kasei Chemicals Corporation | ジアルキルカーボネートとジオールの製造方法 |
| WO2006001256A1 (ja) * | 2004-06-25 | 2006-01-05 | Asahi Kasei Chemicals Corporation | 芳香族カーボネートの工業的製造法 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105194899A (zh) * | 2015-10-16 | 2015-12-30 | 青岛科技大学 | 一种分离甲苯-异丁苯混合物的变径精馏装置及方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20090054676A1 (en) | 2009-02-26 |
| KR101002863B1 (ko) | 2010-12-21 |
| JP4260212B2 (ja) | 2009-04-30 |
| EP1967508B1 (en) | 2013-11-13 |
| WO2007074664A1 (ja) | 2007-07-05 |
| CN101346340A (zh) | 2009-01-14 |
| EP1967508A4 (en) | 2010-12-29 |
| BRPI0620605A2 (pt) | 2012-07-24 |
| JPWO2007074664A1 (ja) | 2009-06-04 |
| IN2008KN00869A (enrdf_load_stackoverflow) | 2008-11-28 |
| CN101346340B (zh) | 2012-03-28 |
| BRPI0620605B1 (pt) | 2016-06-21 |
| KR20080072936A (ko) | 2008-08-07 |
| EA200800919A1 (ru) | 2008-08-29 |
| US8049028B2 (en) | 2011-11-01 |
| EP1967508A1 (en) | 2008-09-10 |
| TWI314549B (en) | 2009-09-11 |
| TW200734299A (en) | 2007-09-16 |
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